ClearanceBrief
510(k) K801653 ยท IYX Camera, Scintillation (Gamma)

MAXI CAMERA 37

ApplicantGeneral Electric Co., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 20, 1980
ReceivedJul 18, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801653

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.